Abstract

The looping of polymers such as DNA is a fundamental process in the molecular biology of living cells, whose interior is characterised by a high degree of molecular crowding. We here investigate in detail the looping dynamics of flexible polymer chains in the presence of different degrees of crowding. From the analysis of the looping-unlooping rates and the looping probabilities of the chain ends we show that the presence of small crowders typically slows down the chain dynamics but larger crowders may in fact facilitate the looping. We rationalise these non-trivial and often counterintuitive effects of the crowder size on the looping kinetics in terms of an effective solution viscosity and standard excluded volume. It is shown that for small crowders the effect of an increased viscosity dominates, while for big crowders we argue that confinement effects (caging) prevail. The tradeoff between both trends can thus result in the impediment or facilitation of polymer looping, depending on the crowder size. We also examine how the crowding volume fraction, chain length, and the attraction strength of the contact groups of the polymer chain affect the looping kinetics and hairpin formation dynamics. Our results are relevant for DNA looping in the absence and presence of protein mediation, DNA hairpin formation, RNA folding, and the folding of polypeptide chains under biologically relevant high-crowding conditions.

Highlights

  • Molecular reactions in living biological cells are running off in a highly complex environment, that is compartmentalised by membrane structures and crowded with macromolecules and structural cytoskeletal networks

  • We study the end-to-end joining statistics; the implications of Macromolecular crowding (MMC) on looping kinetics of inner polymer monomers is beyond the scope of this study and will be presented elsewhere

  • We examine the kinetics of loop closure and opening as functions of the details of the crowders such as the crowding fraction and crowder size

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Summary

Introduction

Molecular reactions in living biological cells are running off in a highly complex environment, that is compartmentalised by membrane structures and crowded with macromolecules and structural cytoskeletal networks. It is known that MMC generally facilitates the association of proteins via volume exclusion effects and favours more compact states.[21] Polymer looping, involves the diffusion of an extended and chain length-dependent fragment of the polymer in crowded solutions. This non-locality effect renders the trends of the inhibition or facilitation of polymer looping kinetics in the presence of MMC less intuitive. Well, due to the competition between depletion effects facilitating looping and an increased effective solution viscosity slowing down the looping kinetics, see Fig. 1 and 2

Model and methods
Potentials and approximations
Parameters and data analysis
Results: crowding and polymer dynamics
Looping probability and polymer size
Looping and unlooping times
Comparison with DNA hairpin formation experiments
Length dependence and effective diffusivity
Effects of the binding affinity
Cavity and caging
Subdiffusion of polymer ends
Diffusion of a tracer particle
Discussion
Abbreviations
Full Text
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